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Lancaster Laboratories – The Company
Lancaster Laboratories is a leading contract analytical laboratory. We provide a broad range of chemistry and microbiology testing services to clients in the pharmaceutical, biotech, medical device, and animal health industries. Among our services are microbiology testing, stability testing and storage, raw materials testing, and analytical method development and validation.

Founded in 1961, we have become a recognized leader in contract analytical laboratory services because of our technical expertise, superlative service, and rigorous compliance with applicable regulations. Nine of the world's largest pharmaceutical companies use our contract
analytical laboratory services. Most importantly, we have a reputation for delivering our data on time, regardless of project size.
Our People
Our chemists and microbiologists combine years of experience in the pharmaceutical industry with a strict adherence to cGMP requirements and a strong commitment to client service. Each project has an assigned project team, including scientists and a project manager, to make sure that it is completed according to our clients’ requirements.
All new employees complete in-house developed training modules in laboratory techniques and core courses in quality and ethics. Once on board, our staff members are kept abreast of cutting-edge technology through extensive in-house training programs and refresher courses in cGMPs and GLPs.
Our Facility
 Lancaster Laboratories is housed in a modern 175,000-square foot facility equipped with state-of-the-art equipment. We offer:
- a 9,000-square-foot controlled microbiology laboratory for all microbiology testing services. This dedicated space includes a sterility test suite that has two 2-half-suit workstation isolators, four transfer isolators, an autoclave isolator integrated with a GMP sterilizer and three VHP 1000 units.
- a separate limited-access building containing 19,500-cubic feet of stability chamber space for storage of stability testing samples.
- a full array of spectrophotometric capabilities (LC/MS/MS, GC/MS, ICP/MS) and chromatographic capabilities (HPLC, GC, IC) for sophisticated pharmaceutical testing and analytical method development and validation.
- dissolution using USP Apparatus 1, 2, 3, 4, and 5.
- a controlled-access and temperature/humidity-monitored sample storage area.
Quality Systems
Our Quality Assurance Program delivers the highest quality of data that is capable of withstanding the rigors of regulatory review. We ensure reliable results through our stringent compliance with cGMP requirements, extensive experience in working with regulatory agencies, and working cooperatively with the client on OOS investigations. |

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Address
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Lancaster Laboratories, Inc. |
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2425 New Holland Pike
PO Box 12425
Lancaster
PA 17605-2425
USA |
| Tel. |
+1 717 656 2300 |
| Fax |
+1 717 656 2681 |

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